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rs879253782

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879253782(A;C)
Make rs879253782(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112707523
GeneAPC
is asnp
is mentioned by
dbSNPrs879253782
ebirs879253782
HLIrs879253782
Exacrs879253782
Varsomers879253782
Maprs879253782
PheGenIrs879253782
hapmaprs879253782
1000 genomesrs879253782
hgdprs879253782
ensemblrs879253782
gopubmedrs879253782
geneviewrs879253782
scholarrs879253782
googlers879253782
pharmgkbrs879253782
gwascentralrs879253782
openSNPrs879253782
23andMers879253782
23andMe allrs879253782
SNP Nexus

SNPshotrs879253782
SNPdbers879253782
MSV3drs879253782
GWAS Ctlgrs879253782
Max Magnitude0
ClinVar
Risk rs879253782(C;C)
Alt rs879253782(C;C)
Reference rs879253782(A;A)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112043220A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000234986.1,